Tag Archives: housebound
Experiences of living with severe CFS/ME
Experiences of living with severe Chronic Fatigue Syndrome/Myalgic Encephalomyelitis, by Victoria Strassheim, Julia L Newton and Tracy Collins in Healthcare 2021, 9(2), 168 [doi.org/10.3390/healthcare9020168] (This article belongs to the Special Issue ME/CFS – the Severely and Very Severely Affected) Research … Continue reading
Homebound versus bedridden status among those with ME/CFS
Homebound versus bedridden status among those with Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome, by Karl Conroy, Shaun Bhatia, Mohammed Islam and Leonard A Jason in Healthcare 2021, 9(2), 106 [doi.org/10.3390/healthcare9020106] (This article belongs to the Special Issue ME/CFS – the Severely and … Continue reading
Health Care responsibility & compassion-visiting the housebound patient severely affected by ME/CFS
Health Care responsibility and compassion-visiting the housebound patient severely affected by ME/CFS, by Caroline Kingdon, Dionysius Giotas, Luis Nacul and Eliana Lacerda in Healthcare 2020, 8(3), 197 [doi.org/10.3390/healthcare8030197] [This article belongs to the Special Issue ME/CFS – the Severely and … Continue reading
Being a housebound digital academic
The Sociological review blog post, by Anna Wood, 17 November 2017: Being a Housebound Digital Academic I have been housebound with a chronic health condition (Myalgic Encephalomyelitis, ME) since 2008. Yet over the last few years I’ve published three papers and … Continue reading
Housebound people with ME have greater physical impairment
Research abstract: Objectives: The objective of this study was to examine individuals with myalgic encephalomyelitis and chronic fatigue syndrome who are confined to their homes due to severe symptomatology. The existing literature fails to address differences between this group, and less severe, nonhousebound patient … Continue reading
